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首页> 外文期刊>Journal of proteome research >Quantitative Characterization of the Neuropeptide Level Changes in Dorsal Horn and Dorsal Root Ganglia Regions of the Murine Itch Models
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Quantitative Characterization of the Neuropeptide Level Changes in Dorsal Horn and Dorsal Root Ganglia Regions of the Murine Itch Models

机译:鼠痒模型背角和背根神经节区域的神经肽水平变化的定量表征

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Chronic itch can be extremely devastating and, in many cases, difficult to treat. One challenge in treating itch disorders is the limited understanding of the multitude of chemical players involved in the communication of itch sensation from the peripheral to the central nervous system. Neuropeptides are intercellular signaling molecules that are known to be involved in the transmission of itch signals from primary afferent neurons, which detect itch in the skin, to higher-order circuits in the spinal cord and brain. To investigate the role of neuropeptides in transmitting itch signals, we generated two mouse models of chronic itch-Acetone-Ether-Water (AEW, dry skin) and calcipotriol (MC903, atopic dermatitis). For peptide identification and quantitation, we analyzed the peptide content of dorsal root ganglia (DRG) and dorsal horn (DH) tissues from chronically itchy mice using liquid chromatography coupled to tandem mass spectrometry. De novo-assisted database searching facilitated the identification and quantitation of 335 peptides for DH MC903, 318 for DH AEW, 266 for DRG MC903, and 271 for DRG AEW. Of these quantifiable peptides, we detected 30 that were differentially regulated in the tested models, after accounting for multiple testing correction (q <= 0.1). These include several peptide candidates derived from neuropeptide precursors, such as proSAAS, protachykinin-1, proenkephalin, and calcitonin gene-related peptide, some of them previously linked to itch. The peptides identified in this study may help elucidate our understanding about these debilitating disorders. Data are available via ProteomeXchange with identifier PXD015949.
机译:慢性瘙痒可能是非常毁灭性的,并且在许多情况下,难以治疗。治疗瘙痒症的一个挑战是对众多化学品玩家的挑战是有限的,参与从周边到中枢神经系统的瘙痒感的传播的众多化学品。神经疏皮肽是已知从初级传入神经元的瘙痒信号传递的细胞间信号传递分子,其检测皮肤中的瘙痒,到脊髓和脑中的高阶电路。为了探讨神经肽在传递瘙痒信号中的作用,我们产生了两种小鼠模型的慢性瘙痒 - 丙酮 - 醚 - 水(AEV,Dird Skin)和Calcipotriol(MC903,Atopic皮炎)。对于肽鉴定和定量,通过使用液相色谱法与串联质谱法一起分析从慢性瘙痒小鼠的背根神经节(DRG)和背角(DH)组织的肽含量。 DE Novo辅助数据库搜索促进了DH MC903,318的335肽的识别和定量,用于DRG MC903,266,271用于DRG EEV。在这些可量化的肽中,在考虑多次测试校正后,我们检测到在测试模型中差异调节的30(Q <= 0.1)。这些包括衍生自神经肽前体的几种肽候选者,例如Prosaas,protachykin-1,前藻素和钙蛋白基因相关肽,其中一些先前与瘙痒相关联。本研究中确定的肽可能有助于阐明我们对这些衰弱障碍的理解。数据可通过Proteomexchange提供标识符PXD015949。

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